Active Tuberculosis Is Associated with Depletion of HIV-Specific CD4 and CD8 T Cells in People with HIV.

IF 1.5 4区 医学 Q4 IMMUNOLOGY AIDS research and human retroviruses Pub Date : 2024-07-01 Epub Date: 2024-03-14 DOI:10.1089/AID.2023.0088
Jeremiah Khayumbi, Loren E Sasser, Taryn A McLaughlin, Benson Muchiri, Joshua Ongalo, Joan Tonui, Samuel Gurrion Ouma, Angie Campbell, Felix Hayara Odhiambo, Chelimo Kiprotich, Neel R Gandhi, Cheryl L Day
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Abstract

Infection with Mycobacterium tuberculosis (Mtb) in people with HIV (PWH) is associated with depletion of Mtb-specific CD4 T cell responses, increased risk of progression to active tuberculosis (TB) disease, and increased immune activation. Although higher HIV viral loads have been reported in Mtb/HIV co-infection, the extent to which Mtb infection and TB disease impact the frequency and phenotype of HIV-specific T cell responses has not been well described. We enrolled a cohort of PWH in Kenya across a spectrum of Mtb infection states, including those with no evidence of Mtb infection, latent Mtb infection (LTBI), and active pulmonary TB disease, and evaluated the frequency, immune activation, and cytotoxicity phenotype of HIV-specific CD4 and CD8 T cell responses in peripheral blood by flow cytometry. We found evidence of depletion of HIV-specific CD4 and CD8 T cells in people with TB, but not with LTBI. Expression of the immune activation markers human leukocyte antigen-DR isotype (HLA-DR) and Ki67 and of the cytotoxic molecules granzyme B and perforin were increased in total CD4 and CD8 T cell populations in individuals with TB, although expression of these markers by HIV-specific CD4 and CD8 T cells did not differ by Mtb infection status. These data suggest that TB is associated with overall increased T cell activation and cytotoxicity and with depletion of HIV-specific CD4 and CD8 T cells, which may contribute to further impairment of T cell-mediated immune control of HIV replication in the setting of TB.

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活动性结核病与艾滋病毒感染者体内艾滋病毒特异性 CD4 和 CD8 T 细胞的消耗有关。
艾滋病病毒感染者(PWH)感染结核分枝杆菌(Mtb)与Mtb特异性CD4 T细胞反应耗竭、发展为活动性结核病(TB)的风险增加以及免疫激活增加有关。虽然有报道称Mtb/HIV合并感染时HIV病毒载量较高,但Mtb感染和结核病对HIV特异性T细胞反应的频率和表型的影响程度尚未得到很好的描述。我们在肯尼亚招募了一批不同Mtb感染状态的PWH,包括无Mtb感染证据、潜伏Mtb感染(LTBI)和活动性肺结核病患者,并通过流式细胞术评估了外周血中HIV特异性CD4和CD8 T细胞反应的频率、免疫激活和细胞毒性表型。我们发现,在肺结核患者中,有证据表明艾滋病毒特异性 CD4 和 CD8 T 细胞耗竭,而在肺结核患者中则没有发现。在肺结核患者的 CD4 和 CD8 T 细胞群中,免疫激活标志物 HLA-DR 和 Ki67 的表达以及细胞毒性分子颗粒酶 B 和穿孔素的表达均有所增加,尽管 HIV 特异性 CD4 和 CD8 T 细胞对这些标志物的表达并不因 Mtb 感染状态而异。这些数据表明,肺结核与 T 细胞活化和细胞毒性的整体增加以及艾滋病毒特异性 CD4 和 CD8 T 细胞的耗竭有关,这可能会在肺结核的情况下进一步损害 T 细胞介导的对艾滋病毒复制的免疫控制。
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来源期刊
CiteScore
3.10
自引率
6.70%
发文量
201
审稿时长
3-6 weeks
期刊介绍: AIDS Research and Human Retroviruses was the very first AIDS publication in the field over 30 years ago, and today it is still the critical resource advancing research in retroviruses, including AIDS. The Journal provides the broadest coverage from molecular biology to clinical studies and outcomes research, focusing on developments in prevention science, novel therapeutics, and immune-restorative approaches. Cutting-edge papers on the latest progress and research advances through clinical trials and examination of targeted antiretroviral agents lead to improvements in translational medicine for optimal treatment outcomes. AIDS Research and Human Retroviruses coverage includes: HIV cure research HIV prevention science - Vaccine research - Systemic and Topical PreP Molecular and cell biology of HIV and SIV Developments in HIV pathogenesis and comorbidities Molecular biology, immunology, and epidemiology of HTLV Pharmacology of HIV therapy Social and behavioral science Rapid publication of emerging sequence information.
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